chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8115512383115512384CT19GENICheterozygous926054902
8115513030115513031CT10GENICheterozygous926054903
8115516330115516331CCG73GENICheterozygous926095281
8115518076115518077AG25GENICheterozygous926054904
8115519250115519251GA16GENICheterozygous926054905
8115523834115523835AG35GENICheterozygous926054906
8115539897115539898TTG6GENICheterozygous926095282
8115541589115541590AAG18GENICheterozygous926095283
8115555931115555932CT59GENICheterozygous926054907
8115557483115557484AG11GENICheterozygous926054908
8115559439115559440AG22GENICheterozygous926054909
8115570286115570287TTC47GENICheterozygous926095284
8115575447115575448TC38GENICheterozygous926054910
8115579013115579014TTGG18GENICheterozygous926095285
8115580541115580542GA17GENICheterozygous926054911
8115583695115583696CT33GENICheterozygous926054912
8115592854115592855AG14GENICheterozygous926054913
8115622540115622541AC28GENICheterozygous926054914
8115623017115623018CT21GENICheterozygous926054915
8115632953115632954CT36GENICheterozygous926054916
8115635013115635014GA13GENICheterozygous926054917
8115639625115639626TA8GENICheterozygous926054918
8115641601115641602AAC41GENICheterozygous926095286